Della Rosa Pasquale Anthony, Cerami Chiara, Gallivanone Francesca, Prestia Annapaola, Caroli Anna, Castiglioni Isabella, Gilardi Maria Carla, Frisoni Giovanni, Friston Karl, Ashburner John, Perani Daniela
Institute of Molecular Bioimaging and Physiology, National Research Council, Segrate, MI, Italy,
Neuroinformatics. 2014 Oct;12(4):575-93. doi: 10.1007/s12021-014-9235-4.
[18F]-fluorodeoxyglucose (FDG) Positron Emission Tomography (PET) is a widely used diagnostic tool that can detect and quantify pathophysiology, as assessed through changes in cerebral glucose metabolism. [18F]-FDG PET scans can be analyzed using voxel-based statistical methods such as Statistical Parametric Mapping (SPM) that provide statistical maps of brain abnormalities in single patients. In order to perform SPM, a "spatial normalization" of an individual's PET scan is required to match a reference PET template. The PET template currently used for SPM normalization is based on [15O]-H2O images and does not resemble either the specific metabolic features of [18F]-FDG brain scans or the specific morphological characteristics of individual brains affected by neurodegeneration. Thus, our aim was to create a new [18F]-FDG PET aging and dementia-specific template for spatial normalization, based on images derived from both age-matched controls and patients. We hypothesized that this template would increase spatial normalization accuracy and thereby preserve crucial information for research and diagnostic purposes. We investigated the statistical sensitivity and registration accuracy of normalization procedures based on the standard and new template-at the single-subject and group level-independently for subjects with Mild Cognitive Impairment (MCI), probable Alzheimer's Disease (AD), Frontotemporal lobar degeneration (FTLD) and dementia with Lewy bodies (DLB). We found a significant statistical effect of the population-specific FDG template-based normalisation in key anatomical regions for each dementia subtype, suggesting that spatial normalization with the new template provides more accurate estimates of metabolic abnormalities for single-subject and group analysis, and therefore, a more effective diagnostic measure.
[18F] - 氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)是一种广泛使用的诊断工具,它可以通过脑葡萄糖代谢的变化来检测和量化病理生理学。[18F] - FDG PET扫描可以使用基于体素的统计方法进行分析,如统计参数映射(SPM),该方法可为单个患者提供脑异常的统计图。为了进行SPM,需要对个体的PET扫描进行“空间归一化”,以匹配参考PET模板。目前用于SPM归一化的PET模板基于[15O] - H2O图像,既不像[18F] - FDG脑扫描的特定代谢特征,也不像受神经退行性变影响的个体大脑的特定形态特征。因此,我们的目标是基于年龄匹配的对照和患者的图像,创建一个新的用于空间归一化的[18F] - FDG PET衰老和痴呆特异性模板。我们假设这个模板将提高空间归一化的准确性,从而为研究和诊断目的保留关键信息。我们分别在单受试者和组水平上,针对轻度认知障碍(MCI)、可能的阿尔茨海默病(AD)、额颞叶变性(FTLD)和路易体痴呆(DLB)患者,研究了基于标准模板和新模板的归一化程序的统计敏感性和配准准确性。我们发现,基于特定人群FDG模板的归一化在每种痴呆亚型的关键解剖区域都有显著的统计效果,这表明使用新模板进行空间归一化可为单受试者和组分析提供更准确的代谢异常估计,因此是一种更有效的诊断措施。